Clinical and Genetic Characteristics of 153 Chinese Patients With X-Linked Hypophosphatemia

X-linked hypophosphatemia (XLH) is caused by inactivating mutations in the phosphate-regulating endopeptidase homolog, X-linked (PHEX) gene, resulting in an excess of circulating intact fibroblast growth factor-23 (iFGF-23) and a waste of renal phosphate. In the present study, we retrospectively rev...

Descripción completa

Detalles Bibliográficos
Autores principales: Lin, Xiaoyun, Li, Shanshan, Zhang, Zhenlin, Yue, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204109/
https://www.ncbi.nlm.nih.gov/pubmed/34141703
http://dx.doi.org/10.3389/fcell.2021.617738

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204109/
https://www.ncbi.nlm.nih.gov/pubmed/34141703
http://dx.doi.org/10.3389/fcell.2021.617738

Ejemplares similares